Canonical Allele Identifier: CA2830544352

Gene: NCAPG2

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.158693556_158693557insTTTTGATGACATTATGAAAAGG , CM000669.2:g.158693556_158693557insTTTTGATGACATTATGAAAAGG	GRCh38
NC_000007.13:g.158486248_158486249insTTTTGATGACATTATGAAAAGG , CM000669.1:g.158486248_158486249insTTTTGATGACATTATGAAAAGG	GRCh37
NC_000007.12:g.158179009_158179010insTTTTGATGACATTATGAAAAGG	NCBI36
NG_047159.1:g.16275_16276insCCTTTTCATAATGTCATCAAAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356309.8:c.79-60_79-59insCCTTTTCATAATGTCATCAAAA MANE Select	ENSP00000348657.3:n.79-60_79-59insCCTTTTCATAATGTCATCAAAA
ENST00000356309.7:c.79-60_79-59insCCTTTTCATAATGTCATCAAAA	ENSP00000348657.3:n.79-60_79-59insCCTTTTCATAATGTCATCAAAA
ENST00000409339.3:c.79-60_79-59insCCTTTTCATAATGTCATCAAAA	ENSP00000387007.3:n.79-60_79-59insCCTTTTCATAATGTCATCAAAA
ENST00000409423.5:c.79-60_79-59insCCTTTTCATAATGTCATCAAAA	ENSP00000386569.1:n.79-60_79-59insCCTTTTCATAATGTCATCAAAA
ENST00000432615.5:c.79-60_79-59insCCTTTTCATAATGTCATCAAAA	ENSP00000414337.1:n.79-60_79-59insCCTTTTCATAATGTCATCAAAA
ENST00000621338.1:n.512-60_512-59insCCTTTTCATAATGTCATCAAAA
NM_001281932.1:c.79-60_79-59insCCTTTTCATAATGTCATCAAAA	NP_001268861.1:n.79-60_79-59insCCTTTTCATAATGTCATCAAAA
NM_001281933.1:c.79-60_79-59insCCTTTTCATAATGTCATCAAAA	NP_001268862.1:n.79-60_79-59insCCTTTTCATAATGTCATCAAAA
NM_017760.6:c.79-60_79-59insCCTTTTCATAATGTCATCAAAA	NP_060230.5:n.79-60_79-59insCCTTTTCATAATGTCATCAAAA
NR_104054.1:n.380-60_380-59insCCTTTTCATAATGTCATCAAAA
XM_005249547.2:c.79-60_79-59insCCTTTTCATAATGTCATCAAAA	XP_005249604.1:n.79-60_79-59insCCTTTTCATAATGTCATCAAAA
XM_011516356.1:c.79-60_79-59insCCTTTTCATAATGTCATCAAAA	XP_011514658.1:n.79-60_79-59insCCTTTTCATAATGTCATCAAAA
XM_011516357.1:c.79-60_79-59insCCTTTTCATAATGTCATCAAAA	XP_011514659.1:n.79-60_79-59insCCTTTTCATAATGTCATCAAAA
XM_011516358.1:c.79-60_79-59insCCTTTTCATAATGTCATCAAAA	XP_011514660.1:n.79-60_79-59insCCTTTTCATAATGTCATCAAAA
XM_005249547.3:c.79-60_79-59insCCTTTTCATAATGTCATCAAAA	XP_005249604.1:n.79-60_79-59insCCTTTTCATAATGTCATCAAAA
XM_011516356.3:c.79-60_79-59insCCTTTTCATAATGTCATCAAAA	XP_011514658.1:n.79-60_79-59insCCTTTTCATAATGTCATCAAAA
XM_011516357.2:c.79-60_79-59insCCTTTTCATAATGTCATCAAAA	XP_011514659.1:n.79-60_79-59insCCTTTTCATAATGTCATCAAAA
XM_011516358.3:c.79-60_79-59insCCTTTTCATAATGTCATCAAAA	XP_011514660.1:n.79-60_79-59insCCTTTTCATAATGTCATCAAAA
XM_017012374.2:c.79-60_79-59insCCTTTTCATAATGTCATCAAAA	XP_016867863.1:n.79-60_79-59insCCTTTTCATAATGTCATCAAAA
XM_017012375.2:c.79-60_79-59insCCTTTTCATAATGTCATCAAAA	XP_016867864.1:n.79-60_79-59insCCTTTTCATAATGTCATCAAAA
XM_017012376.2:c.79-60_79-59insCCTTTTCATAATGTCATCAAAA	XP_016867865.1:n.79-60_79-59insCCTTTTCATAATGTCATCAAAA
NM_001281932.2:c.79-60_79-59insCCTTTTCATAATGTCATCAAAA	NP_001268861.1:n.79-60_79-59insCCTTTTCATAATGTCATCAAAA
NM_001281933.2:c.79-60_79-59insCCTTTTCATAATGTCATCAAAA	NP_001268862.1:n.79-60_79-59insCCTTTTCATAATGTCATCAAAA
NM_017760.7:c.79-60_79-59insCCTTTTCATAATGTCATCAAAA MANE Select	NP_060230.5:n.79-60_79-59insCCTTTTCATAATGTCATCAAAA
NR_104054.2:n.353-60_353-59insCCTTTTCATAATGTCATCAAAA